Aboud M, Shoor R, Salzberg S
J Gen Virol. 1980 Dec;51(Pt 2):431-4. doi: 10.1099/0022-1317-51-2-431.
The effect of human fibroblast interferon (IFN), a heterologous IFN, on the uncoating of murine leukaemia virus (MLV) was investigated in exogenously infected NIH/3T3 mouse cells. Virus uncoating was determined by following the disappearance of the penetrating virus particles from the cytoplasm of the infected cells. Intracellular virus particles were estimated by sedimenting them at high speed from the cytoplasmic fraction of the infected cells and assaying their reverse transcriptase activity. In untreated control cells, uncoating started immediately after penetration, but in cells treated with human IFN, uncoating was delayed for 2 to 3 h. This delay led to prolongation of the infectious cycle, with delayed release of progeny virus. The delay in release did not result from inhibition by IFN of the process of release, since in NIH/3T3 cells chronically infected with MLV, treatment with IFN had no effect on virus release.
在体外感染的NIH/3T3小鼠细胞中,研究了异源干扰素——人成纤维细胞干扰素(IFN)对小鼠白血病病毒(MLV)脱壳的影响。通过追踪感染细胞细胞质中穿透性病毒颗粒的消失来确定病毒脱壳情况。通过从感染细胞的细胞质部分高速沉淀细胞内病毒颗粒并检测其逆转录酶活性来估计细胞内病毒颗粒数量。在未处理的对照细胞中,脱壳在穿透后立即开始,但在用人类IFN处理的细胞中,脱壳延迟了2至3小时。这种延迟导致感染周期延长,子代病毒释放延迟。释放延迟并非由IFN对释放过程的抑制所致,因为在长期感染MLV的NIH/3T3细胞中,用IFN处理对病毒释放没有影响。